These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 7705182)

  • 21. CGHPRO -- a comprehensive data analysis tool for array CGH.
    Chen W; Erdogan F; Ropers HH; Lenzner S; Ullmann R
    BMC Bioinformatics; 2005 Apr; 6():85. PubMed ID: 15807904
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cytogenetic analysis by chromosome painting.
    Carter NP
    Cytometry; 1994 Mar; 18(1):2-10. PubMed ID: 8082483
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Comparative genomic hybridization as a new method for detection of genomic imbalance].
    Ostroverkhova NV; Nazarenko SA; Cheremnykh AD
    Genetika; 2002 Feb; 38(2):149-60. PubMed ID: 11898606
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Integration of conventional cytogenetics, comparative genomic hybridisation and interphase fluorescence in situ hybridisation for the detection of genomic rearrangements in acute leukaemia.
    McGrattan P; Campbell S; Cuthbert R; Jones FG; McMullin MF; Humphreys M
    J Clin Pathol; 2008 Aug; 61(8):903-8. PubMed ID: 18474541
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
    Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
    Cancer Res; 1998 Dec; 58(24):5859-65. PubMed ID: 9865746
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rapid prenatal diagnosis of Down syndrome using quantitative fluorescence in situ hybridization on interphase nuclei.
    Truong K; Gibaud A; Dupont JM; Guilly MN; Soussaline F; Dutrillaux B; Malfoy B
    Prenat Diagn; 2003 Feb; 23(2):146-51. PubMed ID: 12575023
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions.
    Fritz B; Hallermann C; Olert J; Fuchs B; Bruns M; Aslan M; Schmidt S; Coerdt W; Müntefering H; Rehder H
    Eur J Hum Genet; 2001 Jul; 9(7):539-47. PubMed ID: 11464246
    [TBL] [Abstract][Full Text] [Related]  

  • 28. CGH-Profiler: data mining based on genomic aberration profiles.
    Schubert F; Tausch B; Joos S; Eils R
    BMC Bioinformatics; 2005 Jul; 6():188. PubMed ID: 16042799
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.
    Naus NC; van Drunen E; de Klein A; Luyten GP; Paridaens DA; Alers JC; Ksander BR; Beverloo HB; Slater RM
    Genes Chromosomes Cancer; 2001 Mar; 30(3):267-73. PubMed ID: 11170284
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of chromosomal imbalances in transitional cell carcinoma of the bladder by comparative genomic hybridization.
    Voorter C; Joos S; Bringuier PP; Vallinga M; Poddighe P; Schalken J; du Manoir S; Ramaekers F; Lichter P; Hopman A
    Am J Pathol; 1995 Jun; 146(6):1341-54. PubMed ID: 7778674
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Multicolor fluorescence in situ hybridization (mFISH].
    Michalová K; Zemanová Z; Brezinová J
    Cas Lek Cesk; 2001 Mar; 140(4):99-103. PubMed ID: 11284431
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.
    Veldman T; Vignon C; Schröck E; Rowley JD; Ried T
    Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular cytogenetic analysis of head and neck squamous cell carcinoma: By comparative genomic hybridization, spectral karyotyping, and expression array analysis.
    Squire JA; Bayani J; Luk C; Unwin L; Tokunaga J; MacMillan C; Irish J; Brown D; Gullane P; Kamel-Reid S
    Head Neck; 2002 Sep; 24(9):874-87. PubMed ID: 12211052
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping.
    Macville M; Schröck E; Padilla-Nash H; Keck C; Ghadimi BM; Zimonjic D; Popescu N; Ried T
    Cancer Res; 1999 Jan; 59(1):141-50. PubMed ID: 9892199
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
    Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.
    Selvarajah S; Yoshimoto M; Ludkovski O; Park PC; Bayani J; Thorner P; Maire G; Squire JA; Zielenska M
    Cytogenet Genome Res; 2008; 122(1):5-15. PubMed ID: 18931480
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Rapid fluorescence in situ hybridization with repetitive DNA probes: quantification by digital image analysis.
    Celeda D; Aldinger K; Haar FM; Hausmann M; Durm M; Ludwig H; Cremer C
    Cytometry; 1994 Sep; 17(1):13-25. PubMed ID: 8001456
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromosomal imbalances: a hallmark of tumour relapse in primary cutaneous CD30+ T-cell lymphoma.
    Prochazkova M; Chevret E; Beylot-Barry M; Sobotka J; Vergier B; Delaunay M; Turmo M; Ferrer J; Kuglik P; Merlio JP
    J Pathol; 2003 Nov; 201(3):421-9. PubMed ID: 14595754
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chromosomal Alterations in Hepatocellular Carcinoma Cell Lines Detected by Comparative Genomic Hybridization.
    Park SJ; Ha MJ; Kim HC; Kim HJ
    Cancer Res Treat; 2002 Jun; 34(3):175-85. PubMed ID: 26680860
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma cell line MG-63.
    Lim G; Karaskova J; Vukovic B; Bayani J; Beheshti B; Bernardini M; Squire JA; Zielenska M
    Cancer Genet Cytogenet; 2004 Sep; 153(2):158-64. PubMed ID: 15350306
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.